Department of Hematopathology, Advanced Centre for Treatment and Research in Cancer, Tata Memorial Centre, Mumbai, India.
Homi Bhabha National Institute (HBNI), Mumbai, India.
Int J Lab Hematol. 2021 Dec;43(6):1531-1538. doi: 10.1111/ijlh.13680. Epub 2021 Aug 13.
Juvenile myelomonocytic leukemia (JMML) is a rare childhood neoplasm (<5% cases), which has been categorized under myelodysplastic/myeloproliferative neoplasms (MDS/MPN) in the recent classification by the World Health Organization.
We developed a 51-gene (151.5kB) low-cost targeted myeloid panel based on single-molecule molecular inversion probes to comprehensively evaluate the genomic profile of Juvenile myelomonocytic leukemia (JMML).
A total of 50 children with clinical and pathological features of JMML were sequenced at high coverage. Among the 50 patients, 44(88%) harbored mutations in one of the RAS/MAPK-pathway genes, most frequently in NRAS (32%), followed by PTPN11 (28%) and NF1 (22%). One-fifth of children had more than one mutation, with 5 cases harboring two RAS pathway mutations. Monosomy 7 was detected in 32% (16) patients, and five of these did not harbor any RAS pathway mutations. Children with monosomy 7 showed shorter overall survival compared with their wild-type counterparts (P = .02).
Our study highlights that comprehensive genomic profiling identifies at least one mutation in almost 90% of JMML patients. Performing genomic analysis at baseline might help in triaging children with JMML for allogenic stem cell transplant in resource-constrained settings.
幼年髓单核细胞白血病(JMML)是一种罕见的儿童肿瘤(<5%病例),在世界卫生组织最近的分类中被归类为骨髓增生异常/骨髓增殖性肿瘤(MDS/MPN)。
我们开发了一个基于单分子分子反转探针的 51 基因(151.5kB)低成本靶向髓系面板,以全面评估幼年髓单核细胞白血病(JMML)的基因组特征。
共有 50 名具有 JMML 临床和病理特征的儿童进行了高覆盖率测序。在 50 名患者中,44 名(88%)携带 RAS/MAPK 通路基因之一的突变,最常见的是 NRAS(32%),其次是 PTPN11(28%)和 NF1(22%)。五分之一的儿童有不止一个突变,其中 5 例携带两个 RAS 通路突变。有 32%(16 例)的患者存在单体 7,其中 5 例没有携带任何 RAS 通路突变。与野生型相比,单体 7 的儿童总体生存率更短(P=.02)。
我们的研究表明,综合基因组分析可在近 90%的 JMML 患者中确定至少一个突变。在资源有限的环境中,在基线进行基因组分析可能有助于对 JMML 儿童进行同种异体干细胞移植的分类。